Data / Medical devices / Japan / Micron Corp.
Micron Corp.: FDA-registered device maker in OTA-KU Tokyo, Japan, 5 510(k) clearances
Micron Corp. is registered with the FDA (registration 9614726) in OTA-KU Tokyo, Japan. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 8, 2018. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 9614726
- FEI number
- 3002820248
- Address
- 2-17-7 Ikgami, OTA-KU Tokyo, Japan, 146-0082
- Owner or operator
- MICRON CORP. (9037104)
- Roles
- Manufacturer
- First device listed
- December 6, 2007
- Registered through
- 2027
- Brand names listed
- AW-100, M-Tip, Micron SSS, Quick Jet M, SA-100, TA-100, TA-200, VIP60 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| File, Pulp Canal, Endodontic | EKS | 1 | Manufacturer | accessdata.fda.gov |
| Handpiece, Air-Powered, Dental | EFB | 1 | Manufacturer | accessdata.fda.gov |
| Scaler, Ultrasonic | ELC | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Periodontic, Endodontic, Irrigating | EIC | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 8, 2018 | K171150 | AW-100 | ELC | Substantially Equivalent | Micron Corporation | accessdata.fda.gov |
| December 22, 2016 | K161639 | Y-MIC | ELC | Substantially Equivalent | Micron Corporation | accessdata.fda.gov |
| March 28, 2014 | K133170 | QUICK JET M | EFB | Substantially Equivalent | Micron Corp. | accessdata.fda.gov |
| November 20, 2003 | K032995 | SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL) | ELC | Substantially Equivalent | Micron Corp. | accessdata.fda.gov |
| October 18, 1999 | K991239 | VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2 | ELC | Substantially Equivalent | Micron Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Scaler, Ultrasonic
- All makers of File, Pulp Canal, Endodontic
- All makers of Syringe, Periodontic, Endodontic, Irrigating
- All makers of Handpiece, Air-Powered, Dental
Updated March 8, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.